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Published on: October 4, 2018
Cell type specificity of neurovascular coupling in cerebral cortex
Hana Uhlirova1, Kıvılcım Kılıç2, Peifang Tian2,3
1Department of Radiology, University of California, San Diego, La Jolla, United States.
Researchers identified Neuropeptide Y (NPY) released by inhibitory neurons as key in regulating blood flow in the brain. This finding impacts understanding of brain imaging signals and may offer new therapeutic avenues for cerebrovascular diseases.
Area of Science:
- Neuroscience
- Cerebrovascular Physiology
- Neuroimaging
Background:
- Understanding the link between neuronal activity and cerebral blood flow is crucial for interpreting functional Magnetic Resonance Imaging (fMRI) signals.
- Identifying the specific cellular and molecular mechanisms governing cerebrovascular regulation is a key challenge in neuroscience.
Purpose of the Study:
- To elucidate the cellular and molecular mediators of neuronal activity-induced cerebrovascular responses.
- To determine the role of specific neuronal populations in driving cerebral hemodynamics.
- To investigate the implications for Blood Oxygenation Level Dependent (BOLD) fMRI signal interpretation.
Main Methods:
- Utilized optogenetic stimulation in mice to selectively activate cortical excitatory and inhibitory neurons.
- Employed 2-photon imaging to observe real-time vascular responses.
- Investigated the involvement of Neuropeptide Y (NPY) and its Y1 receptors in vasoconstriction.
Main Results:
- Selective activation of cortical excitation and inhibition produced distinct vascular responses.
- Identified Neuropeptide Y (NPY) acting on Y1 receptors as the primary vasoconstrictive mechanism.
- Suggests that NPY-positive inhibitory neurons may significantly contribute to negative BOLD fMRI signals.
Conclusions:
- The NPY-Y1 pathway is a critical regulator of cerebral hemodynamics.
- Task-related negative BOLD signals in the cortex may be largely mediated by NPY-expressing inhibitory neurons.
- The NPY-Y1 pathway presents a potential therapeutic target for cerebrovascular diseases.
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